rs374928784

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs374928784(A;A)

Make rs374928784(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

5082674

Gene

ALG1

is a	snp
is	mentioned by
dbSNP	rs374928784
dbSNP (classic)	rs374928784
ClinGen	rs374928784
ebi	rs374928784
HLI	rs374928784
Exac	rs374928784
Gnomad	rs374928784
Varsome	rs374928784
LitVar	rs374928784
Map	rs374928784
PheGenI	rs374928784
Biobank	rs374928784
1000 genomes	rs374928784
hgdp	rs374928784
ensembl	rs374928784
geneview	rs374928784
scholar	rs374928784
google	rs374928784
pharmgkb	rs374928784
gwascentral	rs374928784
openSNP	rs374928784
23andMe	rs374928784
SNPshot	rs374928784
SNPdbe	rs374928784
MSV3d	rs374928784
GWAS Ctlg	rs374928784

Max Magnitude

0

ClinVar
Risk	rs374928784(A;A)
Alt	rs374928784(A;A)
Reference	Rs374928784(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ALG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.5132675G>A
CLNSRC	ClinVar
CLNACC	RCV000081984.4,